Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 439671Generated: October 27, 2026

1,2-Dibromo-1-chloro-1,2,2-trifluoroethane → 4-Bromo-3-chloro-3,4,4-trifluorobutanoic acid

https://huagongshe.com/reaction/439671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Dibromo-1-chloro-1,2,2-trifluoroethaneHCID 9634—
Reactant3,4,4-Trifluoro-3-butenoic acidHCID 15239174—
CatalystZincHCID 23994—
Product4-Bromo-3-chloro-3,4,4-trifluorobutanoic acidHCID 10912127—

Reaction Steps

A mixture of 1,1,2-trichlorotrifluoroethane (X) (9.37 g, 50 mmol), vinylidene chloride (4.85 g, 50 mmol), ammonium persulfate (11.41 g, 50 mmol), sodium formate (3.4 g, 50 mmol) and water (1.8 g, 0.1 mol) in DMF (80 mL.) was stirred (dry-ice/acetone condensor) at room temperature with air bubbling. After 30 min, an aliquot of the reaction mixture was acidified with dilute HCl, extracted with ether and analyzed by GC, which indicated the formation of two products. These products were identified by GC/MS (EI) as 4-chloro-3,4,4-trifluoro-2-butenoic acid and novel compound 3,4-dichloro-3,4,4-trifluorobutanoic acid (XI). The compound XI gives 3,4,4-trifluoro-3-butenoic add (IV) upon reaction with zinc. Under the above reaction conditions, 1-chloro-1,2-dibromotrifluoroethane (VI) gave 3-chloro-4-bromo-3,4,4-trifluorobutanoic acid (VIII) as one of the products.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05514717
Source datasetuspto-grants-1996_05
ORD IDord-d432447635c04182847b67566a7b2364
Source noteuspto-grants-1996_05